# FDA 483 - MX IMAGING, INC. - April 26, 2023

Source: https://www.globalkeysolutions.net/records/483/mx-imaging-inc/7b6dde1f-7fed-4401-8ebd-a6e5fcb60027

> FDA 483 for MX IMAGING, INC. on April 26, 2023. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: MX IMAGING, INC.
- Inspection Date: 2023-04-26
- Product Type: device
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: MX IMAGING, INC., a medical device manufacturer in Torrance, CA, was cited with two observations during an FDA inspection. The inspection revealed significant deficiencies in the maintenance of both Device History Records and Device Master Records for their CFP 1515 product. These issues indicate a lack of proper documentation for device manufacturing, specifications, and quality assurance.

## Related Officers

- [Albert Rodriguez](https://www.globalkeysolutions.net/people/albert-rodriguez/8bb16dfe-577a-4a8c-a7f0-0fa0404a59cc)

Company: https://www.globalkeysolutions.net/companies/mx-imaging-inc/aadb660d-353c-47d1-8686-e581f2dfc8cd

Office: https://www.globalkeysolutions.net/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6